Terbinafine Hydrochloride 70518-3907
Product NDC
70518-3907- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 3, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA078163
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Terbinafine Hydrochloride | 250 mg/1 |
Drug Class
Allylamine Antifungal [EPC]Allylamine [CS]
Packaging Options(1)
30 TABLET in 1 BLISTER PACK (70518-3907-3)